JohnBoy2000
Bluelighter
- Joined
- May 11, 2016
- Messages
- 2,650
They have a tight binding affinity - specifically olanzapine - with the mACH receptors, and text articles mention it as a potent anti-cholinergic.
Personally, I didn't notice any anti-cholinergic effects with it: urinary retention, dry mouth etc.
Not even sedation.
I was up on 15 - 20 mg.
Slight initial sedation at about 20mg due to its antihistamine action, but that would fade after a couple of hours.
Is it considered a potent anti-cholinergic on a par with say, early tricyclics - amitriptyline etc?
I also didn't experience any weight gain on olanzapine - nor appetite increases, not even for sugars.
Though I do get this with mirtazapine - and it's most welcome.
AP's claimed primary mode of action is D2 antagonism - and that incites sedation?
I'm curious as to why D agonism with say, anti-parkisons agents, is also sedating.
And then dopamine reuptake inhibition is stimulating - with amphetamines and some DNRI's etc?
Baffling....
Personally, I didn't notice any anti-cholinergic effects with it: urinary retention, dry mouth etc.
Not even sedation.
I was up on 15 - 20 mg.
Slight initial sedation at about 20mg due to its antihistamine action, but that would fade after a couple of hours.
Is it considered a potent anti-cholinergic on a par with say, early tricyclics - amitriptyline etc?
I also didn't experience any weight gain on olanzapine - nor appetite increases, not even for sugars.
Though I do get this with mirtazapine - and it's most welcome.
AP's claimed primary mode of action is D2 antagonism - and that incites sedation?
I'm curious as to why D agonism with say, anti-parkisons agents, is also sedating.
And then dopamine reuptake inhibition is stimulating - with amphetamines and some DNRI's etc?
Baffling....
